| scholarly article | Q13442814 |
| P50 | author | Caroline W Sham | Q63661990 |
| P2093 | author name string | Douglas K Bishop | |
| Melissa S McMahill | |||
| P2860 | cites work | The Holliday junction on its thirtieth anniversary | Q24533134 |
| Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae | Q24548535 | ||
| RAD51 is required for the repair of plasmid double-stranded DNA gaps from either plasmid or chromosomal templates | Q24554318 | ||
| ABERRANT RECOMBINATION OF PYRIDOXINE MUTANTS OF Neurospora | Q24560044 | ||
| Recombinational repair of gaps in DNA is asymmetric in Ustilago maydis and can be explained by a migrating D-loop model | Q24605056 | ||
| Mnd1/Hop2 facilitates Dmc1-dependent interhomolog crossover formation in meiosis of budding yeast | Q27930146 | ||
| A pathway for generation and processing of double-strand breaks during meiotic recombination in S. cerevisiae | Q27930541 | ||
| Homothallic switching of yeast mating type cassettes is initiated by a double-stranded cut in the MAT locus | Q27930817 | ||
| The budding yeast Msh4 protein functions in chromosome synapsis and the regulation of crossover distribution | Q27931846 | ||
| DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression | Q27933115 | ||
| Saccharomyces cerevisiae checkpoint genes MEC1, RAD17 and RAD24 are required for normal meiotic recombination partner choice | Q27935546 | ||
| Purification and characterization of the Sgs1 DNA helicase activity of Saccharomyces cerevisiae. | Q27936079 | ||
| Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis | Q27936900 | ||
| Identification of residues in yeast Spo11p critical for meiotic DNA double-strand break formation | Q27938442 | ||
| Meiotic recombination involving heterozygous large insertions in Saccharomyces cerevisiae: formation and repair of large, unpaired DNA loops | Q27939603 | ||
| New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae | Q28131599 | ||
| The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase | Q28170377 | ||
| Differential timing and control of noncrossover and crossover recombination during meiosis | Q28207440 | ||
| The time course and chromosomal localization of recombination-related proteins at meiosis in the mouse are compatible with models that can resolve the early DNA-DNA interactions without reciprocal recombination | Q28214583 | ||
| The repair of double-strand breaks in DNA; a model involving recombination | Q28256950 | ||
| The double-strand-break repair model for recombination | Q28267259 | ||
| Evidence for multiple cycles of strand invasion during repair of double-strand gaps in Drosophila | Q28768697 | ||
| Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method | Q29547550 | ||
| Analysis of wild-type and rad50 mutants of yeast suggests an intimate relationship between meiotic chromosome synapsis and recombination | Q29615272 | ||
| Carbohydrate Metabolism During Ascospore Development in Yeast | Q29616251 | ||
| The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination | Q29618523 | ||
| Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast | Q29618612 | ||
| Mechanism and control of meiotic recombination initiation | Q29618789 | ||
| A mechanism for gene conversion in fungi | Q30052741 | ||
| Identification of double Holliday junctions as intermediates in meiotic recombination. | Q54599520 | ||
| Template switching during break-induced replication | Q56521356 | ||
| Intermediates of Yeast Meiotic Recombination Contain Heteroduplex DNA | Q58486283 | ||
| Gene conversion between duplicated genetic elements in yeast | Q59062391 | ||
| Identification of joint molecules that form frequently between homologs but rarely between sister chromatids during yeast meiosis | Q64389750 | ||
| Extensive 3'-overhanging, single-stranded DNA associated with the meiosis-specific double-strand breaks at the ARG4 recombination initiation site | Q64389995 | ||
| Coconversion of flanking sequences with homothallic switching | Q64390150 | ||
| Meiosis-specific formation of joint DNA molecules containing sequences from homologous chromosomes | Q72722388 | ||
| Crossover interference is abolished in the absence of a synaptonemal complex protein | Q72790781 | ||
| Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1. | Q30827295 | ||
| Detection of heteroduplex DNA molecules among the products of Saccharomyces cerevisiae meiosis. | Q33824887 | ||
| Meiotic recombination between duplicated genetic elements in Saccharomyces cerevisiae. | Q33950787 | ||
| Analysis of meiosis-defective mutations in yeast by physical monitoring of recombination. | Q33952129 | ||
| a/Alpha-specific repression by MAT alpha 2 | Q33954611 | ||
| Analysis of a gene conversion gradient at the HIS4 locus in Saccharomyces cerevisiae | Q33959781 | ||
| Genetic evidence that the meiotic recombination hotspot at the HIS4 locus of Saccharomyces cerevisiae does not represent a site for a symmetrically processed double-strand break | Q33960929 | ||
| Ends-in vs. ends-out recombination in yeast | Q33962081 | ||
| Rearrangements involving repeated sequences within a P element preferentially occur between units close to the transposon extremities | Q33966640 | ||
| A test of the double-strand break repair model for meiotic recombination in Saccharomyces cerevisiae | Q33968364 | ||
| Crossover and noncrossover recombination during meiosis: timing and pathway relationships | Q33988127 | ||
| Expansions and contractions in a tandem repeat induced by double-strand break repair | Q33994800 | ||
| DNA synthesis dependent on genetic recombination: characterization of a reaction catalyzed by purified bacteriophage T4 proteins | Q34162674 | ||
| Molecular genetics of yeast mating type | Q34268647 | ||
| A DNA double chain break stimulates triparental recombination in Saccharomyces cerevisiae | Q34297039 | ||
| Efficient copying of nonhomologous sequences from ectopic sites via P-element-induced gap repair | Q34336201 | ||
| Infrequent co-conversion of markers flanking a meiotic recombination initiation site in Saccharomyces cerevisiae. | Q34572477 | ||
| The conversion gradient at HIS4 of Saccharomyces cerevisiae. I. Heteroduplex rejection and restoration of Mendelian segregation | Q34607928 | ||
| Patterns of Heteroduplex Formation Associated With the Initiation of Meiotic Recombination in the Yeast Saccharomyces cerevisiae | Q34618616 | ||
| Complex minisatellite rearrangements generated in the total or partial absence of Rad27/hFEN1 activity occur in a single generation and are Rad51 and Rad52 dependent. | Q35071154 | ||
| Early decision; meiotic crossover interference prior to stable strand exchange and synapsis | Q35739105 | ||
| DNA homology requirements for mitotic gap repair in Drosophila | Q36098071 | ||
| Timing of molecular events in meiosis in Saccharomyces cerevisiae: stable heteroduplex DNA is formed late in meiotic prophase | Q36659309 | ||
| P-element-induced interallelic gene conversion of insertions and deletions in Drosophila melanogaster | Q36825877 | ||
| Occurrence of crossed strand-exchange forms in yeast DNA during meiosis | Q37337080 | ||
| Tying synaptonemal complex initiation to the formation and programmed repair of DNA double-strand breaks | Q37358029 | ||
| Meiosis: how could it work? | Q37394575 | ||
| The Saccharomyces cerevisiae MER3 gene, encoding a novel helicase-like protein, is required for crossover control in meiosis | Q38319411 | ||
| Measurements of excision repair tracts formed during meiotic recombination in Saccharomyces cerevisiae | Q40678599 | ||
| Conservative inheritance of newly synthesized DNA in double-strand break-induced gene conversion | Q41077128 | ||
| Plasmid-mediated induction of recombination in yeast. | Q41837609 | ||
| The large loop repair and mismatch repair pathways of Saccharomyces cerevisiae act on distinct substrates during meiosis | Q42828810 | ||
| Decreasing gradients of gene conversion on both sides of the initiation site for meiotic recombination at the ARG4 locus in yeast | Q42961993 | ||
| Meiotic gene conversion in yeast tetrads and the theory of recombination. | Q42972056 | ||
| Saccharomyces cerevisiae Mer3 helicase stimulates 3'-5' heteroduplex extension by Rad51; implications for crossover control in meiotic recombination | Q46127945 | ||
| The Sgs1 Helicase Regulates Chromosome Synapsis and Meiotic Crossing Over | Q47388021 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e299 | |
| P577 | publication date | 2007-11-06 | |
| P1433 | published in | PLOS Biology | Q1771695 |
| P1476 | title | Synthesis-dependent strand annealing in meiosis | |
| P478 | volume | 5 |
| Q91603727 | A mutant form of Dmc1 that bypasses the requirement for accessory protein Mei5-Sae3 reveals independent activities of Mei5-Sae3 and Rad51 in Dmc1 filament stability |
| Q64928626 | A mutation in the endonuclease domain of mouse MLH3 reveals novel roles for MutLγ during crossover formation in meiotic prophase I. |
| Q41925429 | A positive but complex association between meiotic double-strand break hotspots and open chromatin in Saccharomyces cerevisiae |
| Q50645139 | A strategy for characterization of persistent heteroduplex DNA in higher plants. |
| Q97519370 | ATM Promotes RAD51-Mediated Meiotic DSB Repair by Inter-Sister-Chromatid Recombination in Arabidopsis |
| Q44780934 | Analysis of crossover breakpoints yields new insights into the nature of the gene conversion events associated with large NF1 deletions mediated by nonallelic homologous recombination |
| Q49911835 | Arabidopsis thaliana FANCD2 Promotes Meiotic Crossover Formation |
| Q28264465 | BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism |
| Q48141083 | Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identification |
| Q37656154 | Control of Meiotic Crossovers: From Double-Strand Break Formation to Designation. |
| Q21144863 | Controlling meiotic recombinational repair - specifying the roles of ZMMs, Sgs1 and Mus81/Mms4 in crossover formation |
| Q26768639 | DNA double-strand break formation and repair in Tetrahymena meiosis |
| Q34931255 | DNA strand exchange and RecA homologs in meiosis |
| Q38342215 | DNA-pairing and annealing processes in homologous recombination and homology-directed repair |
| Q34440683 | Deep genome-wide measurement of meiotic gene conversion using tetrad analysis in Arabidopsis thaliana |
| Q90616013 | Distinct Functions in Regulation of Meiotic Crossovers for DNA Damage Response Clamp Loader Rad24(Rad17) and Mec1(ATR) Kinase |
| Q39957722 | Double Holliday junctions are intermediates of DNA break repair. |
| Q55097912 | Elevated temperature increases meiotic crossover frequency via the interfering (Type I) pathway in Arabidopsis thaliana. |
| Q38344293 | Epigenetic control of meiotic recombination in plants |
| Q33913156 | Evolutionary conservation of meiotic DSB proteins: more than just Spo11 |
| Q21092719 | Frequent and efficient use of the sister chromatid for DNA double-strand break repair during budding yeast meiosis |
| Q36830881 | GC-biased gene conversion in yeast is specifically associated with crossovers: molecular mechanisms and evolutionary significance |
| Q28579624 | Genetic evidence suggests that Spata22 is required for the maintenance of Rad51 foci in mammalian meiosis |
| Q57172482 | Genome wide analysis of meiotic recombination in yeast: For a few SNPs more |
| Q34042733 | Genome-wide analysis of heteroduplex DNA in mismatch repair-deficient yeast cells reveals novel properties of meiotic recombination pathways |
| Q58696735 | HO Endonuclease-Initiated Recombination in Yeast Meiosis Fails To Promote Homologous Centromere Pairing and Is Not Constrained To Utilize the Dmc1 Recombinase |
| Q38325311 | High-throughput plasmid construction using homologous recombination in yeast: its mechanisms and application to protein production for X-ray crystallography |
| Q27939787 | Homologous recombination via synthesis-dependent strand annealing in yeast requires the Irc20 and Srs2 DNA helicases |
| Q59341842 | Hotspots for Initiation of Meiotic Recombination |
| Q36026803 | Identification of Putative Mek1 Substrates during Meiosis in Saccharomyces cerevisiae Using Quantitative Phosphoproteomics |
| Q34588131 | Immunofluorescent characterization of meiotic recombination in human males with variable spermatogenesis |
| Q60957365 | Interhomolog polymorphism shapes meiotic crossover within the Arabidopsis RAC1 and RPP13 disease resistance genes |
| Q36808266 | Isolation of meiotic recombinants from mouse sperm. |
| Q35530032 | Juxtaposition of heterozygous and homozygous regions causes reciprocal crossover remodelling via interference during Arabidopsis meiosis |
| Q37574327 | Local chromosome context is a major determinant of crossover pathway biochemistry during budding yeast meiosis. |
| Q34931212 | Mechanism and regulation of meiotic recombination initiation |
| Q37136141 | Mechanisms of ectopic gene conversion |
| Q64296098 | Meiocyte-Specific and AtSPO11-1-Dependent Small RNAs and Their Association with Meiotic Gene Expression and Recombination |
| Q34122575 | Meiosis in flowering plants and other green organisms |
| Q38618828 | Meiotic Recombination: The Essence of Heredity |
| Q27940335 | Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation |
| Q26991732 | Meiotic development in Caenorhabditis elegans |
| Q38450160 | Meiotic recombination hotspots - a comparative view. |
| Q24597411 | Meiotic versus mitotic recombination: two different routes for double-strand break repair: the different functions of meiotic versus mitotic DSB repair are reflected in different pathway usage and different outcomes |
| Q34340732 | Mek1 kinase governs outcomes of meiotic recombination and the checkpoint response |
| Q37759692 | Metabolism of postsynaptic recombination intermediates |
| Q50420122 | Monitoring Recombination During Meiosis in Budding Yeast |
| Q34396683 | Mouse tetrad analysis provides insights into recombination mechanisms and hotspot evolutionary dynamics |
| Q34707053 | Multiple pathways suppress non-allelic homologous recombination during meiosis in Saccharomyces cerevisiae |
| Q27940287 | Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis. |
| Q35223901 | New and old ways to control meiotic recombination |
| Q33962076 | Nucleosome occupancy landscape and dynamics at mouse recombination hotspots |
| Q33486503 | Pch2 links chromosome axis remodeling at future crossover sites and crossover distribution during yeast meiosis |
| Q38988847 | Pervasive and essential roles of the Top3-Rmi1 decatenase orchestrate recombination and facilitate chromosome segregation in meiosis |
| Q35872885 | Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast Meiosis |
| Q34280906 | Polarized gene conversion at the bz locus of maize |
| Q35619405 | Prelude to a division |
| Q34102182 | RTEL-1 enforces meiotic crossover interference and homeostasis |
| Q34151222 | RTEL1: an essential helicase for telomere maintenance and the regulation of homologous recombination |
| Q36048609 | Rare sex or out of reach equilibrium? The dynamics of F IS in partially clonal organisms |
| Q27939265 | RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination |
| Q36077603 | Recombination Rate Heterogeneity within Arabidopsis Disease Resistance Genes |
| Q36724327 | Sites of recombination are local determinants of meiotic homolog pairing in Saccharomyces cerevisiae |
| Q27317410 | Smc5/6 coordinates formation and resolution of joint molecules with chromosome morphology to ensure meiotic divisions |
| Q28301386 | Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions |
| Q35621644 | The CAF-1 and Hir Histone Chaperones Associate with Sites of Meiotic Double-Strand Breaks in Budding Yeast |
| Q36384393 | The DNA replication factor RFC1 is required for interference-sensitive meiotic crossovers in Arabidopsis thaliana |
| Q28729084 | The fission yeast FANCM ortholog directs non-crossover recombination during meiosis |
| Q64388083 | The meiotic-specific Mek1 kinase in budding yeast regulates interhomolog recombination and coordinates meiotic progression with double-strand break repair |
| Q33486516 | The pch2Delta mutation in baker's yeast alters meiotic crossover levels and confers a defect in crossover interference |
| Q37372408 | The rate of meiotic gene conversion varies by sex and age. |
| Q64386525 | The recombinases DMC1 and RAD51 are functionally and spatially separated during meiosis in Arabidopsis |
| Q43936941 | The synaptonemal complex protein ZYP1 is required for imposition of meiotic crossovers in barley |
| Q37914029 | The template choice decision in meiosis: is the sister important? |
| Q28474239 | Topoisomerase 3alpha and RMI1 suppress somatic crossovers and are essential for resolution of meiotic recombination intermediates in Arabidopsis thaliana |
| Q21092401 | Transmission distortion affecting human noncrossover but not crossover recombination: a hidden source of meiotic drive |
| Q33728150 | Trying to Avoid Your Sister |
| Q27929966 | Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination. |
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